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Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study
SIMPLE SUMMARY: Uveal melanoma usually shows a liver-dominant metastasis spread. Even in the light of multiple treatment options, including liver-targeted therapies, patients die early from this disease. Two promising treatment options are transarterial radioembolization (SIRT) and chemosaturation-p...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605323/ https://www.ncbi.nlm.nih.gov/pubmed/37894309 http://dx.doi.org/10.3390/cancers15204942 |
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author | Kolb, Manuel Forschner, Andrea Artzner, Christoph Grözinger, Gerd Said, Ines Dittmann, Helmut Seith, Ferdinand |
author_facet | Kolb, Manuel Forschner, Andrea Artzner, Christoph Grözinger, Gerd Said, Ines Dittmann, Helmut Seith, Ferdinand |
author_sort | Kolb, Manuel |
collection | PubMed |
description | SIMPLE SUMMARY: Uveal melanoma usually shows a liver-dominant metastasis spread. Even in the light of multiple treatment options, including liver-targeted therapies, patients die early from this disease. Two promising treatment options are transarterial radioembolization (SIRT) and chemosaturation-percutaneous hepatic perfusion (CS-PHP), and in this study, we retrospectively compared their efficiency on 62 patients (SIRT = 34, CS-PHP = 28) receiving multiple treatment cycles. By a standardized evaluation of the tumor response using RECIST 1.1, we saw a disease control rate of 18% for SIRT and in 30% for CS-PHP. The median of progression-free survival was 127.5 days for SIRT and 408.5 days for CS-PHP, and advanced analysis showed this to be not significant. The median overall survival after treatment was 300.5 days for SIRT and 516 days for CS-PHP, and advanced analysis showed this to be significant. We conclude that for these patients, CS-PHP might therefore be preferable. ABSTRACT: Even with liver-targeted therapies, uveal melanoma with hepatic metastasis remains a challenge. The aim of this study was to compare the outcome of patients treated with either SIRT or CS-PHP. We included 62 patients with hepatic metastasized uveal melanoma (n = 34 with SIRT, receiving 41 cycles; n = 28 with CS-PHP, receiving 56 cycles) that received their treatments between 12/2013 and 02/2020 at a single center. We evaluated their response according to the RECIST 1.1, as well as progression-free survival (PFS) and overall survival (OS), after the initiation of the first cycle of the liver-directed treatment using Cox regression, adjusted via propensity score analysis for confounders, including the amount of hepatic involvement. The disease control rate was 18% for SIRT and 30% for CS-PHP. The median (range) of PFS was 127.5 (19–1912) days for SIRT and 408.5 (3–1809) days for CS-PHP; adjusted Cox regression showed no significant difference (p = 0.090). The median (range) of OS was 300.5 (19–1912) days for SIRT and 516 (5–1836) days for CS-PHP; adjusted Cox regression showed a significant difference (p = 0.006). In our patient cohort, patients treated with CS-PHP showed a significantly longer OS than patients treated with SIRT. CS-PHP might therefore be preferable for patients with liver-dominant metastatic uveal melanoma. |
format | Online Article Text |
id | pubmed-10605323 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106053232023-10-28 Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study Kolb, Manuel Forschner, Andrea Artzner, Christoph Grözinger, Gerd Said, Ines Dittmann, Helmut Seith, Ferdinand Cancers (Basel) Article SIMPLE SUMMARY: Uveal melanoma usually shows a liver-dominant metastasis spread. Even in the light of multiple treatment options, including liver-targeted therapies, patients die early from this disease. Two promising treatment options are transarterial radioembolization (SIRT) and chemosaturation-percutaneous hepatic perfusion (CS-PHP), and in this study, we retrospectively compared their efficiency on 62 patients (SIRT = 34, CS-PHP = 28) receiving multiple treatment cycles. By a standardized evaluation of the tumor response using RECIST 1.1, we saw a disease control rate of 18% for SIRT and in 30% for CS-PHP. The median of progression-free survival was 127.5 days for SIRT and 408.5 days for CS-PHP, and advanced analysis showed this to be not significant. The median overall survival after treatment was 300.5 days for SIRT and 516 days for CS-PHP, and advanced analysis showed this to be significant. We conclude that for these patients, CS-PHP might therefore be preferable. ABSTRACT: Even with liver-targeted therapies, uveal melanoma with hepatic metastasis remains a challenge. The aim of this study was to compare the outcome of patients treated with either SIRT or CS-PHP. We included 62 patients with hepatic metastasized uveal melanoma (n = 34 with SIRT, receiving 41 cycles; n = 28 with CS-PHP, receiving 56 cycles) that received their treatments between 12/2013 and 02/2020 at a single center. We evaluated their response according to the RECIST 1.1, as well as progression-free survival (PFS) and overall survival (OS), after the initiation of the first cycle of the liver-directed treatment using Cox regression, adjusted via propensity score analysis for confounders, including the amount of hepatic involvement. The disease control rate was 18% for SIRT and 30% for CS-PHP. The median (range) of PFS was 127.5 (19–1912) days for SIRT and 408.5 (3–1809) days for CS-PHP; adjusted Cox regression showed no significant difference (p = 0.090). The median (range) of OS was 300.5 (19–1912) days for SIRT and 516 (5–1836) days for CS-PHP; adjusted Cox regression showed a significant difference (p = 0.006). In our patient cohort, patients treated with CS-PHP showed a significantly longer OS than patients treated with SIRT. CS-PHP might therefore be preferable for patients with liver-dominant metastatic uveal melanoma. MDPI 2023-10-11 /pmc/articles/PMC10605323/ /pubmed/37894309 http://dx.doi.org/10.3390/cancers15204942 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kolb, Manuel Forschner, Andrea Artzner, Christoph Grözinger, Gerd Said, Ines Dittmann, Helmut Seith, Ferdinand Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study |
title | Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study |
title_full | Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study |
title_fullStr | Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study |
title_full_unstemmed | Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study |
title_short | Selective Internal Radiotherapy (SIRT) and Chemosaturation Percutaneous Hepatic Perfusion (CS-PHP) for Metastasized Uveal Melanoma: A Retrospective Comparative Study |
title_sort | selective internal radiotherapy (sirt) and chemosaturation percutaneous hepatic perfusion (cs-php) for metastasized uveal melanoma: a retrospective comparative study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10605323/ https://www.ncbi.nlm.nih.gov/pubmed/37894309 http://dx.doi.org/10.3390/cancers15204942 |
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